EP2161349B1 - Method for producing a copper-based white alloy for producing naturally antibacterial articles - Google Patents
Method for producing a copper-based white alloy for producing naturally antibacterial articles Download PDFInfo
- Publication number
- EP2161349B1 EP2161349B1 EP09008026.8A EP09008026A EP2161349B1 EP 2161349 B1 EP2161349 B1 EP 2161349B1 EP 09008026 A EP09008026 A EP 09008026A EP 2161349 B1 EP2161349 B1 EP 2161349B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- cold
- copper
- alloy
- subjecting
- semifinished article
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
- 229910045601 alloy Inorganic materials 0.000 title claims description 57
- 239000000956 alloy Substances 0.000 title claims description 57
- 239000010949 copper Substances 0.000 title claims description 29
- 229910052802 copper Inorganic materials 0.000 title claims description 27
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 title claims description 25
- 230000000844 anti-bacterial effect Effects 0.000 title claims description 13
- 238000004519 manufacturing process Methods 0.000 title claims description 7
- 239000011572 manganese Substances 0.000 claims description 31
- 229910052748 manganese Inorganic materials 0.000 claims description 25
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 18
- 238000000137 annealing Methods 0.000 claims description 13
- 239000010410 layer Substances 0.000 claims description 12
- 238000001953 recrystallisation Methods 0.000 claims description 10
- 238000011282 treatment Methods 0.000 claims description 10
- 229910052782 aluminium Inorganic materials 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 239000012535 impurity Substances 0.000 claims description 8
- 230000009467 reduction Effects 0.000 claims description 8
- 239000011701 zinc Substances 0.000 claims description 8
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 7
- 238000001125 extrusion Methods 0.000 claims description 7
- 239000002344 surface layer Substances 0.000 claims description 7
- 229910052725 zinc Inorganic materials 0.000 claims description 7
- 238000005275 alloying Methods 0.000 claims description 6
- 230000001680 brushing effect Effects 0.000 claims description 6
- 238000005266 casting Methods 0.000 claims description 6
- 230000036541 health Effects 0.000 claims description 6
- 235000013305 food Nutrition 0.000 claims description 5
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 4
- 238000003754 machining Methods 0.000 claims description 4
- 238000003801 milling Methods 0.000 claims description 4
- 238000005096 rolling process Methods 0.000 claims description 4
- 230000003068 static effect Effects 0.000 claims description 4
- 229910052718 tin Inorganic materials 0.000 claims description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 16
- 239000010935 stainless steel Substances 0.000 description 16
- 229910000881 Cu alloy Inorganic materials 0.000 description 15
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 11
- 239000000463 material Substances 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- 229910052759 nickel Inorganic materials 0.000 description 8
- 229910017566 Cu-Mn Inorganic materials 0.000 description 6
- 229910017871 Cu—Mn Inorganic materials 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 238000005482 strain hardening Methods 0.000 description 6
- 241001275902 Parabramis pekinensis Species 0.000 description 5
- 239000004411 aluminium Substances 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- 229910000831 Steel Inorganic materials 0.000 description 4
- 230000003373 anti-fouling effect Effects 0.000 description 4
- 230000000845 anti-microbial effect Effects 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 239000000645 desinfectant Substances 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 244000052769 pathogen Species 0.000 description 4
- 239000010959 steel Substances 0.000 description 4
- 238000004659 sterilization and disinfection Methods 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 229910000914 Mn alloy Inorganic materials 0.000 description 3
- HPDFFVBPXCTEDN-UHFFFAOYSA-N copper manganese Chemical compound [Mn].[Cu] HPDFFVBPXCTEDN-UHFFFAOYSA-N 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 238000005098 hot rolling Methods 0.000 description 3
- 229910052742 iron Inorganic materials 0.000 description 3
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 244000005700 microbiome Species 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000012925 reference material Substances 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 241000588724 Escherichia coli Species 0.000 description 2
- 101001013832 Homo sapiens Mitochondrial peptide methionine sulfoxide reductase Proteins 0.000 description 2
- 241000186779 Listeria monocytogenes Species 0.000 description 2
- 102100031767 Mitochondrial peptide methionine sulfoxide reductase Human genes 0.000 description 2
- 229910000990 Ni alloy Inorganic materials 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 239000002519 antifouling agent Substances 0.000 description 2
- 230000001580 bacterial effect Effects 0.000 description 2
- 238000010622 cold drawing Methods 0.000 description 2
- 238000005097 cold rolling Methods 0.000 description 2
- 238000001816 cooling Methods 0.000 description 2
- 230000005518 electrochemistry Effects 0.000 description 2
- 238000011534 incubation Methods 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 229910052745 lead Inorganic materials 0.000 description 2
- 230000000813 microbial effect Effects 0.000 description 2
- 230000005012 migration Effects 0.000 description 2
- 238000013508 migration Methods 0.000 description 2
- 230000001717 pathogenic effect Effects 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000013535 sea water Substances 0.000 description 2
- 239000011265 semifinished product Substances 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
- 230000002588 toxic effect Effects 0.000 description 2
- 230000000007 visual effect Effects 0.000 description 2
- 229920001817 Agar Polymers 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910052684 Cerium Inorganic materials 0.000 description 1
- 229910000798 CuZn10 Inorganic materials 0.000 description 1
- 229910000570 Cupronickel Inorganic materials 0.000 description 1
- 241001646719 Escherichia coli O157:H7 Species 0.000 description 1
- GYHNNYVSQQEPJS-UHFFFAOYSA-N Gallium Chemical compound [Ga] GYHNNYVSQQEPJS-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- 241000588915 Klebsiella aerogenes Species 0.000 description 1
- RJQXTJLFIWVMTO-TYNCELHUSA-N Methicillin Chemical compound COC1=CC=CC(OC)=C1C(=O)N[C@@H]1C(=O)N2[C@@H](C(O)=O)C(C)(C)S[C@@H]21 RJQXTJLFIWVMTO-TYNCELHUSA-N 0.000 description 1
- 229910001122 Mischmetal Inorganic materials 0.000 description 1
- 241000589517 Pseudomonas aeruginosa Species 0.000 description 1
- 229910000589 SAE 304 stainless steel Inorganic materials 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 241000191967 Staphylococcus aureus Species 0.000 description 1
- 229910000537 White brass Inorganic materials 0.000 description 1
- 229910001361 White metal Inorganic materials 0.000 description 1
- 229910001297 Zn alloy Inorganic materials 0.000 description 1
- HEWIALZDOKKCSI-UHFFFAOYSA-N [Ni].[Zn].[Mn].[Cu] Chemical compound [Ni].[Zn].[Mn].[Cu] HEWIALZDOKKCSI-UHFFFAOYSA-N 0.000 description 1
- 230000001464 adherent effect Effects 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 229940088710 antibiotic agent Drugs 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 244000052616 bacterial pathogen Species 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 239000006285 cell suspension Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 230000003750 conditioning effect Effects 0.000 description 1
- 230000008602 contraction Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 229940092559 enterobacter aerogenes Drugs 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 235000012438 extruded product Nutrition 0.000 description 1
- 229910052733 gallium Inorganic materials 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 239000010437 gem Substances 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 238000011086 high cleaning Methods 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 238000009533 lab test Methods 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229960003085 meticillin Drugs 0.000 description 1
- 244000000010 microbial pathogen Species 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000011369 optimal treatment Methods 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001846 repelling effect Effects 0.000 description 1
- 238000005204 segregation Methods 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- PORWMNRCUJJQNO-UHFFFAOYSA-N tellurium atom Chemical compound [Te] PORWMNRCUJJQNO-UHFFFAOYSA-N 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
- 229910000832 white gold Inorganic materials 0.000 description 1
- 239000010938 white gold Substances 0.000 description 1
- 239000010969 white metal Substances 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/08—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of copper or alloys based thereon
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C9/00—Alloys based on copper
- C22C9/05—Alloys based on copper with manganese as the next major constituent
Definitions
- the present invention relates to a method for producing articles made of a copper-based white alloy, wherein these articles are naturally antibacterial and simultaneously have an excellent mechanical resistance, an easy machinability, a high cleaning ease and an appearance similar to that of stainless steel.
- copper and brasses have aesthetical and technological features which are generally considered inappropriate to validly replace stainless steel, for instance in the manufacturing of articles such as sanitaryware, sinks, tables, working surfaces for canteens or laboratories, basins for sanitary use, lockers, both because the mechanical features are typically much poorer than those of stainless steel, and because they are not white, but are instead of different colours such as red, pink and yellow.
- the use of copper and alloys thereof in the health field has been for the time being limited to components intended to remain hidden, for instance those of hydraulic or conditioning systems, such as finned heat exchangers.
- manganese may have a whitening effect on copper similar to that of nickel
- the only known white alloys which do not contain nickel and are not brasses are the so-called “manganins", used for manufacturing electrical resistors due to the low conductivity manganese imparts alloyed copper, already from a few percentage points.
- the examined alloys have a Cu-Mn-combination of 70:30.
- the examples comprise Zn and Al.
- CA 964 408 A1 discloses a method comprising casting a plate based on a Cu-alloy and comprising 30% Mn. A hot rolling from three inches to 0.35 inch is performed followed by cold rolling from 0.35 to 0.1 inch. It follows an annealing procedure for 1 h at 600 - 750°C for recrystallization.
- DE 1 224 937 B refers to the use of copper alloys.
- the disclosed copper alloys may be used for bearings according to their friction properties.
- the alloy contains up to 8% aluminum, up to 5% Ni and up to 45% Zn. Further the alloy contains Tellur, Silicium and up to 12% Mangan.
- the alloy may be subject of hot forming or cold forming and annealing between 200 and 700°C for recrystallization. This document does not deal with articles that have antibacterial properties.
- WO 00/68447 A discloses a copper alloy with a golden visual appearance.
- the material has a transverse electrical conductivities substantially similar to that of copper alloy C713 and when clad to a copper alloy C110 core, a transverse electrical conductivities substantially similar to both sides of a Susan-B.-Anthony-US-Dollar coin.
- the copper base alloy is a copper-manganese-zink-nickel alloy consisting for example by weight of 10-15% Zn, 7-12% Mn, 2-6% Ni or 10-14% Zn, 5-10% Mn, 2-6% Ni, optionally controlled contents of Cr, Al, Fe, P, the balance being Cu with inevitable impurities.
- planchet is stamped from the clad material
- the planchet is annealed prior to coining.
- the suitable annealing profile is 700°C for 15-20 minutes in an atmosphere of 96% by volume, of nitrogen and 4%, by volume, of hydrogen or other combustible gas mixtures.
- the copper alloys were hot rolled to a thickness of 0.5 inch, milled to remove oxides and then cold rolled to 0.03 inch and buffed to provide a constant surface finish.
- a copper alloy treated by this method has a golden visual appearance.
- the invention relates to the method of claim 1 for producing articles, these articles being in particular intended to be employed in the health and/or food field, these articles being provided with intrinsic antibacterial properties.
- the manganese, and possible other alloying elements, except for impurities are present in an amount such as to determine machinability, colour and surface properties of the alloy similar to those of stainless steel and simultaneously intrinsic antibacterial properties of the articles on respective exposed surfaces thereof.
- the employed alloy does not contain aluminium, except as an impurity and neither zinc nor other alloying elements, but exclusively manganese and copper.
- Tin in case it is required, may also be contained as further alloying element, but again in very low percentages, preferably below 2% so as not to produce in use the segregation of precipitates or low-melting phases which impart fragility to the alloy.
- said alloy exclusively contains, except for impurities, copper and manganese, copper being prevailing.
- the content of manganese ranges, in any case, in varying percentages between 15% and up to 40% by weight and preferably in an amount such as to obtain a crystalline structure of the alloy, exclusively in alpha phase, at ambient temperature.
- the optimal nominal composition of the alloy according to the use of the invention is 80% copper and 20% manganese.
- composition of the alloy according to the use of the invention is in any case such as to display on the surface antibacterial properties directed at least against microorganisms selected from the group consisting of: E.coli, MSRA, Listeria monocytogenes.
- the method of the invention comprises the steps of:
- the alloy contains manganese in a varying weight percentage between 15% and 40% and does not contain aluminium, and preferably neither zinc, except as impurities.
- the first and second predetermined percentages of sectional reduction are on the order of 90% and the step of complete re-crystallization annealing of the cold semifinished article is performed at a temperature ranging between 550°C and 750°C and for about 4 hours, if performed in a static furnace or for a total time of about 45 minutes, if performed in a tunnel type furnace.
- a step of abrasive brushing is performed so as to remove a surface layer of the cold annealed semifinished article having a thickness of about 4 microns.
- the antibacterial properties of copper alloys experimentally tested on many different bacterial strains are probably due to the surface migration, and therefore on the exposed surfaces of articles made with these alloys, of copper atoms, a migration that is interrupted by the presence of aluminium in the alloy.
- the presence of aluminium in the alloy, unless the latter is present only as an impurity (the presence of impurities is in any case inevitable) must be avoided.
- Plate P88501 was then used, due to its better quality (chemical composition identical to the nominal composition - 80% copper and 20% manganese).
- the plate was subjected to a hot rolling process bringing it to 740°C for 3.5 hours and was subsequently rolled thus obtaining in subsequent steps a reduction in the section of about 90%; the thickness was in particular reduced from 115 mm to 10 mm in 8 steps, thus reaching a final temperature of about 660-670°; the hot-rolled product was cooled down to about 350°C before forcedly cooling down to ambient temperature with water.
- the rolled product was then examined and analysed to detect the depth and nature of the surface layers oxidised and depleted of alloying elements (manganese).
- Table 2 Thickness of the oxidising layers measured on both sides of the longitudinal section of Cu80Mn20 hot-rolled plate
- Top - edge 1 Mean MAX. m MIN. m ST.DEV. m Side A 25.48 73.71 3.98 18.65 Side B 24.28 47.81 10.76 9.09
- Top - edge 2 Mean m MAX. m MIN. m ST.DEV.
- the depth of the detected layers of oxidation and depletion of Mn were relatively high and discontinuous, but such that said layers could easily and totally be removed by the normal milling/scalping operations which are generally performed after hot-rolling.
- the hot-rolled product after the milling/scalping operation and subsequent removal of the oxidised layers and with depletion of manganese, was subjected to a cold-rolling operation, again obtaining a reduction in the section of about 90% (from 10 to 0.7 mm of thickness) in subsequent steps, with the consequent work hardening and increase of hardness.
- the cold-rolled product was then subjected to a heat annealing treatment in a static furnace in a reducing atmosphere at 600°C for 4 hours for the re-crystallization. This treatment has been selected on the basis of a series of laboratory tests at different temperatures, in order to identify the optimal treatment, as shown in table 4.
- Table 4 Structure and size of the grain of Cu80Mn20 samples after one hour of heat treatment at increasing temperatures.
- Mean size of the grain (mm) Heat treatment 1 mm thickness 0.5 mm thickness 400 °C / 1 hour Fibrous structure Fibrous structure 450 °C / 1 hour Fibrous structure Fibrous structure 500 °C / 1 hour Re-crystallization start Re-crystallization start 550 °C / 1 hour 0.005 0.0075 600°C / 1 hour 0.0075 0.0075 650 °C / 1 hour 0.010 0.015
- the depletion involves a layer which is no more than 4-5 microns, which may easily be removed with a common operation of abrasive brushing after the heat treatment.
- the tested CuMn20 alloy is suitable to replace the stainless steel in any application, such as the manufacture of furniture, tools, work surfaces, etc., having a considerable hardness and high mechanical resistance, well beyond those of brasses.
- the antimicrobial properties of three different copper alloys were compared, and specifically the CuMn20 alloy (alloy 3) according to the invention, previously prepared according to the previous examples, a CuSn6Zn6 alloy (alloy 2) and a CuZn10 alloy (alloy 1), with two different reference materials and specifically DHP copper AISI 304 steel (stainless steel).
- sample specimens were incubated at 37°C.
- the test was repeated 6 times, varying the time of contact in incubation.
- Each sample specimen was tested for the following times: 0, 5, 10, 20, 40 and 80 minutes.
- the sample specimen was recovered and treated with an aqueous solution to remove the pathogens; the solution was then diluted and incorporated in agar and a microscopical count was finally carried out on the survived microbial cells.
- the antimicrobial activity of the previously prepared and machined alloy, CuMn20 is substantially very similar to that of copper DHP against all of the tested pathogenic microorganisms, while stainless steel is substantially devoid thereof.
- the antimicrobial activity of the CuMn20 alloy is also comparable (or better), with the content of copper being the same, with respect to that of the other tested alloys, which however have a mechanical resistance and hardness that make them unsuitable to replace steel and, especially, do not have a colour comparable to that of steel, while the CuMn20 alloy according to the invention has a white metal colour comparable to that of steel.
- the double-hole extrusion of the ingots was performed so as to obtain wires with a diameter of 26 mm, with a 4000 ton press in a range of extrusion temperatures from 770 to 800 °C, spraying the outputted wires with water coming from appropriate sprayers to limit oxidation of the alloy and/or the depletion of Mn.
- the power absorbed by the press expressed in tons, varies from 2000 to 2300 due to the high mechanical features of the Cu80Mn20 alloy. From the metallographic point of view, the best results both as regards the mean diameter of the grain and as regards the homogeneity thereof, were obtained with an extrusion temperature equivalent to 780°C.
- the wires were subjected to a final step of cold drawing to a 2mm- or 1.80mm-diameter, so as to obtain a work hardening of 7.4% or, respectively, of 25% and therefore give rise, with the same alloy, to a final wire material in a medium-hard or hard physical state.
- the possible brushing ensured the absence of surface layers of oxide or of layers depleted of Mn.
- Billets of Cu80Mn20 alloy were extruded under water to tubes having a 100mm-diameter, 11mm-thickness wall, so as to limit the formation of surface oxides and/or layers depleted of Mn.
- the extrusion of the billet in the form of a tube was performed in a range of extrusion temperatures in the range between 790 and 805°C.
- the power absorbed by the press expressed in bars, was about 290, which is an acceptable value considering the high mechanical features of the Cu80Mn20 alloy.
- a cold plastic deformation processing was performed using a pilgrim mill set at 70 hits/minute with a feed of 11.11 mm until tubes having a 45mm-diameter by a 2.25-wall thickness were obtained and later the semifinished products obtained thereby were subjected to a single operation of rectilinear cold drawing to a 35mm-diameter by 1.90 mm-thickness and a following annealing at 650°C for 4 hours in a reducing atmosphere.
Landscapes
- Chemical & Material Sciences (AREA)
- Mechanical Engineering (AREA)
- Organic Chemistry (AREA)
- Metallurgy (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Crystallography & Structural Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Heat Treatment Of Steel (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
- Adornments (AREA)
- Apparatus For Disinfection Or Sterilisation (AREA)
Description
- The present invention relates to a method for producing articles made of a copper-based white alloy, wherein these articles are naturally antibacterial and simultaneously have an excellent mechanical resistance, an easy machinability, a high cleaning ease and an appearance similar to that of stainless steel.
- It has been known since ancient times (ancient Egypt) that copper has disinfectant properties. More recently, copper and its alloys (brasses) have been investigated for their bactericidal properties on some pathogen microorganisms [H. T. Michels, ASTM Standardization NEWS, October 2006, pp. 29-31] and compared to stainless steel, on the surface of which the same pathogens that manage to survive on copper and alloys thereof only for a few hours, can instead survive30 days or more, in the absence of disinfectant treatment. US-EP approved antimicrobial abilities of tests have shown the copper and brasses against Staphylococcusaureus, Enterobacteraerogenes, E. Coli 0157:H7, Pseudomonas aeruginosa and MRSA (methicillin resistant Stafilococcus aureus).
- However, copper and brasses have aesthetical and technological features which are generally considered inappropriate to validly replace stainless steel, for instance in the manufacturing of articles such as sanitaryware, sinks, tables, working surfaces for canteens or laboratories, basins for sanitary use, lockers, both because the mechanical features are typically much poorer than those of stainless steel, and because they are not white, but are instead of different colours such as red, pink and yellow. For all of these reasons, the use of copper and alloys thereof in the health field has been for the time being limited to components intended to remain hidden, for instance those of hydraulic or conditioning systems, such as finned heat exchangers.
- There are also known, for producing jewels having an appearance similar to silver and for producing accessories for clothes, such as buttons and zips, white copper alloys, such as copper and nickel alloys, which however are nowadays increasingly less used due to the allergising effects of nickel, and the so-called "white brasses" , which are alloys of copper and zinc with the addition of manganese and/or aluminium, which have progressively replaced the previous, such as for instance the alloys disclosed in
EP1306453B1 or inUS6863746B , in the latter case the disclosed alloy being used to perform weldings on articles made of white gold. Although manganese may have a whitening effect on copper similar to that of nickel, the only known white alloys which do not contain nickel and are not brasses, are the so-called "manganins", used for manufacturing electrical resistors due to the low conductivity manganese imparts alloyed copper, already from a few percentage points. - MUKHERJEE, D. ET AL: "Antifouling properties of copper-manganese alloys" TOOL & ALLOY STEELS, 27(9), 287-9 refers an examination of corrosion resistant and antifouling properties of Cu-Mn alloys. It was seen that a right proportion of manganese as well as the inclusion of a rear earth and some exotic material may result in the lowering of corrosion, and at the same time in the liberation of an optimum amount of toxic ion to behave as an anti-fouling agent. The examined alloys have a Cu-Mn-combination of 70:30. The examples comprise Zn and Al. The authors conclude this paper after recording the fact that Ce and Ce-Ga modified CuMn alloys, depend on their medium and environment, which controls their selective properties and their better resistance, as far as corrosion and fouling resistance are concerned. MUKHERJEE, D. ET AL: "SRB-cidal properties of some copper-manganese alloys" BULLETIN OF ELECTROCHEMISTRY, 6(5), 499-500 refers to different copper-manganese alloys that have been fabricated and tested for their antifouling properties in SRB-cultures under static condition. Among the alloys experimented, the Cu-Mn alloy containing misch metal and gallium, besides being excellent antifoulant, acts as an efficient SRB-cide as well. The examined alloys were of the type 70:30 Cu-Mn.
- A further paper dealing with the behavior of Cu-Mn alloys in sea-water is MUKHERJEE, D. ET AL: "Corrosion resistant 5-7, 9-15 and antifouling behavior of Cu-Mn alloys in sea-water" BULLETIN OF ELECTROCHEMISTRY, 9(8-10), 427-9. The authors conclude this study by highlighting the aspect of dual mechanism, observed in some alloyed and modified variety of Cu-Mn system, where the dissolution of toxic ions is probably assisted by the formation of an adherent oxide toxic-film, repelling the formation of the initial slime-layer.
-
CA 964 408 A1 discloses a method comprising casting a plate based on a Cu-alloy and comprising 30% Mn. A hot rolling from three inches to 0.35 inch is performed followed by cold rolling from 0.35 to 0.1 inch. It follows an annealing procedure for 1 h at 600 - 750°C for recrystallization. -
DE 1 224 937 B -
WO 00/68447 A - It is an object of the present invention to therefore allow the replacement of stainless steel for producing articles intended to be employed in the health and/or food field or for which the intrinsic antibacterial properties are in any case important, with a material that has an appearance similar to that of stainless steel, has a low tendency to get dirty, may easily be cleaned with common cleaning products and, especially, has intrinsic antibacterial features, so as not to require frequent disinfection operations which are required instead by stainless steel when used in health and/or food applications.
- It is also an object of the invention to provide a method for producing articles, in particular intended to be employed in the health and/or food field, which are naturally, i.e. intrinsically, provided with antibacterial abilities, so as not to require frequent disinfections of the exposed surfaces.
- The invention relates to the method of
claim 1 for producing articles, these articles being in particular intended to be employed in the health and/or food field, these articles being provided with intrinsic antibacterial properties. - In particular, the manganese, and possible other alloying elements, except for impurities, are present in an amount such as to determine machinability, colour and surface properties of the alloy similar to those of stainless steel and simultaneously intrinsic antibacterial properties of the articles on respective exposed surfaces thereof.
- According to the invention, the employed alloy does not contain aluminium, except as an impurity and neither zinc nor other alloying elements, but exclusively manganese and copper. Tin, in case it is required, may also be contained as further alloying element, but again in very low percentages, preferably below 2% so as not to produce in use the segregation of precipitates or low-melting phases which impart fragility to the alloy.
- In the preferred embodiment, said alloy exclusively contains, except for impurities, copper and manganese, copper being prevailing.
- The content of manganese ranges, in any case, in varying percentages between 15% and up to 40% by weight and preferably in an amount such as to obtain a crystalline structure of the alloy, exclusively in alpha phase, at ambient temperature. The optimal nominal composition of the alloy according to the use of the invention is 80% copper and 20% manganese.
- The composition of the alloy according to the use of the invention is in any case such as to display on the surface antibacterial properties directed at least against microorganisms selected from the group consisting of: E.coli, MSRA, Listeria monocytogenes.
- In particular, the method of the invention comprises the steps of:
- casting a plate or a cylindrical ingot made of a copper-based alloy containing manganese as the main alloying element, in an amount such as to make the alloy white in colour and to impart a crystalline structure in alpha phase at ambient temperature thereto;
- subjecting the plate or ingot to a series of hot plastic deformation machining treatments in sequence (rolling or drawing or extrusion), to obtain a first, predetermined percentage of sectional reduction;
- subjecting the hot semifinished article to a series of cold plastic deformation machining treatments in sequence (rolling or drawing), to obtain a second, predetermined percentage of sectional reduction;
- subjecting the cold semifinished article thus obtained to one or more heat annealing treatments of complete re-crystallization, in a reducing atmosphere;
- subjecting the hot and/or cold semifinished article to at least one step of removing a surface layer thereof with a low manganese contents; and
- obtaining a desired article with the cold annealed semifinished article.
- The alloy contains manganese in a varying weight percentage between 15% and 40% and does not contain aluminium, and preferably neither zinc, except as impurities.
- Furthermore, the first and second predetermined percentages of sectional reduction are on the order of 90% and the step of complete re-crystallization annealing of the cold semifinished article is performed at a temperature ranging between 550°C and 750°C and for about 4 hours, if performed in a static furnace or for a total time of about 45 minutes, if performed in a tunnel type furnace.
- A step of abrasive brushing is performed so as to remove a surface layer of the cold annealed semifinished article having a thickness of about 4 microns.
- Thereby, complex articles such as sinks, basins,tanks, plates, working surfaces of bathroom details,as tables, furniture tops, well as tubes, bars or wires, for instance to produce handrails, handles, knobs, sieves, may be obtained according to the invention and substantially without virtually any scraps, the articles having the appearance of stainless steel and being provided at the same time with very good natural or intrinsic antibacterial properties, which substantially make common sterilisation operations with disinfectants useless or at least redundant. Similar stainless steel articles are usually subjected to these disinfection operations, by the way with results which are always less effective as many bacterial strains have developed a considerable resistance to commonly used disinfectants and to antibiotics and have therefore become a continuous danger, in particular in a hospital environment, such as MRSA or E- coli O157:H7.
- Furthermore, according to the results of the experiments performed by the Applicant, the antibacterial properties of copper alloys experimentally tested on many different bacterial strains, are probably due to the surface migration, and therefore on the exposed surfaces of articles made with these alloys, of copper atoms, a migration that is interrupted by the presence of aluminium in the alloy.
- Therefore, according to the invention, the presence of aluminium in the alloy, unless the latter is present only as an impurity (the presence of impurities is in any case inevitable) must be avoided.
- A preferred embodiment of the invention will now be disclosed by way of mere non-limitative example with reference to the figures of the attached drawings, wherein:
-
figure 1 shows a diagram that compares the mechanical properties of the alloy according to the invention with another copper alloy and with a stainless steel; and -
figures 2 to 4 comparatively show the biological properties of some copper alloys, among which the alloy of the invention, and of stainless steel, for different types of germs. - Further features of the invention will be apparent from the following examples for carrying out the invention.
- Two 900 kg plates were prepared by casting, the plates having dimensions 1800 x 500 x 115 mm (length x width x thickness) and each having the mean composition shown in Table 1.
Table 1 Mean chemical composition Melting N. Cu % Mn % Fe % Ni % Sn % Pb % P 88500 81.2 18.8 0.015 0.03 <0.01 0.01 P 88501 80.0 20.0 0.02 0.035 <0.01 0.01 - Plate P88501 was then used, due to its better quality (chemical composition identical to the nominal composition - 80% copper and 20% manganese).
- The plate was subjected to a hot rolling process bringing it to 740°C for 3.5 hours and was subsequently rolled thus obtaining in subsequent steps a reduction in the section of about 90%; the thickness was in particular reduced from 115 mm to 10 mm in 8 steps, thus reaching a final temperature of about 660-670°; the hot-rolled product was cooled down to about 350°C before forcedly cooling down to ambient temperature with water.
- The rolled product was then examined and analysed to detect the depth and nature of the surface layers oxidised and depleted of alloying elements (manganese).
- The results which were obtained are shown in tables 2 and 3, which follow.
Table 2 Thickness of the oxidising layers measured on both sides of the longitudinal section of Cu80Mn20 hot-rolled plate Top - edge 1Mean MAX. m MIN. m ST.DEV. m Side A 25.48 73.71 3.98 18.65 Side B 24.28 47.81 10.76 9.09 Top - centre Mean MAX. m MIN. m ST.DEV. m SIDE A 13.14 27.52 4.42 6.4 SIDE B 17.23 85.79 3.98 17.7 Top - edge 2Mean m MAX. m MIN. m ST.DEV. m Side A 13.26 28.73 6.78 6.07 Side B 37.75 100 5.18 27.46 Bottom - edge 1Mean m MAX. m MIN. m ST.DEV .m Side A 20.81 41.04 5.98 9.82 Side B 17.42 35.48 6.77 7.39 Bottom - centre Mean m MAX. m MIN. m ST.DEV .m Side A 17.92 39.06 9.57 6.51 Side B 5.45 12.9 3.59 2.26 Bottom - edge 2Mean m MAX. m MIN. m ST.DEV .m Side A 16.91 28.68 7.17 6.58 Side B 39.33 110.05 9.38 29.61 Table 3 Chemical composition along a linear profile (from the outer surface to 17.5 microns deep) Position Top Bottom Edge Centre Edge Centre Wt% Mn wt% Cu wt% Mn wt% Cu wt% mn wt% Cu wt% Mn wt % Cu 0 30 70 58 42 21.7 78.3 44.3 55.7 1.75 12.1 87.9 10.7 89.3 0.5 99.5 8.6 91.4 3.5 18.8 81.2 19.9 80.1 12.3 87.7 17.1 82.9 5.25 20.5 79.5 20.4 79.6 18.2 81.8 19.6 80.4 7 20.7 79.3 20.5 79.5 19.8 80.2 20.5 79.5 8.75 20.3 79.7 20.1 79.9 20.2 79.8 20.8 79.2 10.5 20.3 79.7 23.6 76.4 20.4 79.6 20.4 79.6 12.25 20 80 20.2 79.8 21 79 20.4 79.6 14 20.1 79.9 19.9 80.1 21 79 20.7 79.3 15.75 19.3 80.7 19.9 80.1 21.2 78.8 19.9 80.1 17.5 19.5 80.5 20.2 79.8 21 79 20 80 - As may be appreciated, the depth of the detected layers of oxidation and depletion of Mn were relatively high and discontinuous, but such that said layers could easily and totally be removed by the normal milling/scalping operations which are generally performed after hot-rolling.
- Subsequently, the hot-rolled product, after the milling/scalping operation and subsequent removal of the oxidised layers and with depletion of manganese, was subjected to a cold-rolling operation, again obtaining a reduction in the section of about 90% (from 10 to 0.7 mm of thickness) in subsequent steps, with the consequent work hardening and increase of hardness. The cold-rolled product was then subjected to a heat annealing treatment in a static furnace in a reducing atmosphere at 600°C for 4 hours for the re-crystallization. This treatment has been selected on the basis of a series of laboratory tests at different temperatures, in order to identify the optimal treatment, as shown in table 4.
Table 4 Structure and size of the grain of Cu80Mn20 samples after one hour of heat treatment at increasing temperatures. Mean size of the grain (mm) Heat treatment 1 mm thickness 0.5 mm thickness 400 °C / 1 hour Fibrous structure Fibrous structure 450 °C / 1 hour Fibrous structure Fibrous structure 500 °C / 1 hour Re-crystallization start Re-crystallization start 550 °C / 1 hour 0.005 0.0075 600°C / 1 hour 0.0075 0.0075 650 °C / 1 hour 0.010 0.015 - Test specimens of the rolled material were subjected to the common tests for identifying the mechanical properties, in comparison to reference materials (other copper alloys and stainless steel). The results which were obtained are shown in
figure 1 , where the hardness curves of the different materials are shown as a function of the strain hardening, and in the following tables.Table 5 Material HV E (GPa) Rp(0,2) (MPa) Rm (MPa) A50mm (%) CuMn20 119 118 260 470 32 CuZn20 77 110 115 330 47 AISI 304-316 129 193 205 515 40 Tab.2 Comparison between different materials Table 6 Material IE (mm) IB R (%) H (%) L.D.R. CuMn20 10,6 70 ≅100 4.9 2,12 CuZn20 10,6-12 66-68 ≅96-100 - 1,94-2,00 AISI 304-316 11-12 - ≅50-60* - 2,18-2,25* Tab.3 Formability properties Table 7 Cu80Mn20 Cu80Zn20 Aisi 304 temper Rp (Mpa) Rm (Mpa) Rp (Mpa) Rm (Mpa) Rp (Mpa) Rm (Mpa) Annealed 256 493 115 330 205 515 1/4 Hard 308 498 300 420 413 690 1/2 Hard 564 597 440 510 606 827 Hard 820 860 480 570 772 1020 -
- As may be noted, the depletion involves a layer which is no more than 4-5 microns, which may easily be removed with a common operation of abrasive brushing after the heat treatment.
- From the comparison among the various materials, it may also be noted that the tested CuMn20 alloy is suitable to replace the stainless steel in any application, such as the manufacture of furniture, tools, work surfaces, etc., having a considerable hardness and high mechanical resistance, well beyond those of brasses.
- The antimicrobial properties of three different copper alloys were compared, and specifically the CuMn20 alloy (alloy 3) according to the invention, previously prepared according to the previous examples, a CuSn6Zn6 alloy (alloy 2) and a CuZn10 alloy (alloy 1), with two different reference materials and specifically DHP copper AISI 304 steel (stainless steel).
- Three different pathogen microorganisms were used for the tests, specifically E. coli, MSRA and Listeria monocytogenes.
- Flat sheet sample specimens, made of the tested alloys and of the reference materials, each of a size equivalent to about 5.5 cm2 were treated with 10 microlitres of microbial cell suspension in water, having a concentration of about 108 cell units per millilitre.
- Subsequently, the sample specimens were incubated at 37°C. The test was repeated 6 times, varying the time of contact in incubation. Each sample specimen was tested for the following times: 0, 5, 10, 20, 40 and 80 minutes.
- After each incubation step was finished, the sample specimen was recovered and treated with an aqueous solution to remove the pathogens; the solution was then diluted and incorporated in agar and a microscopical count was finally carried out on the survived microbial cells.
- The results which were obtained are shown in
figures 2 ,3 and 4 . - As may be noted, the antimicrobial activity of the previously prepared and machined alloy, CuMn20 is substantially very similar to that of copper DHP against all of the tested pathogenic microorganisms, while stainless steel is substantially devoid thereof. The antimicrobial activity of the CuMn20 alloy is also comparable (or better), with the content of copper being the same, with respect to that of the other tested alloys, which however have a mechanical resistance and hardness that make them unsuitable to replace steel and, especially, do not have a colour comparable to that of steel, while the CuMn20 alloy according to the invention has a white metal colour comparable to that of steel.
- Four cylindrical ingots were prepared having a diameter of 305 mm using standard copper ingot moulds with an inner graphite insert so as to render less drastic the cooling of the metal in the ingot mould and therefore avoid the formation of contraction cracks. The metal was taken to a temperature of 1140°C in the melting furnace and, after the analytical controls to verify the adherence to the nominal composition, was poured in the holding furnace; the casting started when the metal reached the temperature of 1100 °C.
- The chemical composition resulting from the mean of the two samples of cast withdrawn respectively at the beginning and at the end of each casting is shown in table 9.
Table 9 Mean chemical composition of the cylindrical ingots in Cu80Mn20. Melting N. Cu % Mn % Fe % Ni % Sn % Pb % L88277 80.9 19.04 0.025 0.032 <0.01 <0.01 L88278 79.8 20.10 0.012 0.028 <0.01 0.01 L88279 79.5 20.40 0.017 0.039 <0.01 0.01 L88280 79.7 20.20 0.020 0.035 <0.01 <0.01 - Subsequently, the double-hole extrusion of the ingots was performed so as to obtain wires with a diameter of 26 mm, with a 4000 ton press in a range of extrusion temperatures from 770 to 800 °C, spraying the outputted wires with water coming from appropriate sprayers to limit oxidation of the alloy and/or the depletion of Mn. In these conditions the power absorbed by the press, expressed in tons, varies from 2000 to 2300 due to the high mechanical features of the Cu80Mn20 alloy. From the metallographic point of view, the best results both as regards the mean diameter of the grain and as regards the homogeneity thereof, were obtained with an extrusion temperature equivalent to 780°C. Later, the extruded products were rolled to a diameter of 20 mm and an annealing was performed for 3 hours at 650°C in a reducing atmosphere. Different cold plastic deformation (drawing) operations were then performed from a semifinished product having a 20mm-diameter to a wire having a 2.08mm-diameter, performing an intermediate step of milling from 5.70 to 5.30 mm to remove the layers of oxidation and depletion of Mn, the depth of which was less than that identified for the corresponding layers of example 1 for the rolled products. Finally, after a complete re-crystallization annealing performed at 650°C for 3 hours in a reducing atmosphere, the wires were subjected to a final step of cold drawing to a 2mm- or 1.80mm-diameter, so as to obtain a work hardening of 7.4% or, respectively, of 25% and therefore give rise, with the same alloy, to a final wire material in a medium-hard or hard physical state. As a final step, the possible brushing ensured the absence of surface layers of oxide or of layers depleted of Mn.
- The values of the mechanical features which may be obtained by means of the drawing operations, depending on the different possible strain hardening, are shown in table 10.
Table 10 Summary of the mean values of Rm, Rp and HV measured during the cold plastic deformation cycle as a function of the percentage strain hardening the Cu80Mn20 wire undergoes. Strain hardening Rm MPa Rp MPa HV 500g/15" 0 490 240 150 7.4 540 310 170 25 717 450 195 37 790 580 215 55 827 710 235 85 875 835 250 - Billets of Cu80Mn20 alloy were extruded under water to tubes having a 100mm-diameter, 11mm-thickness wall, so as to limit the formation of surface oxides and/or layers depleted of Mn.
- The extrusion of the billet in the form of a tube was performed in a range of extrusion temperatures in the range between 790 and 805°C. In these conditions, the power absorbed by the press, expressed in bars, was about 290, which is an acceptable value considering the high mechanical features of the Cu80Mn20 alloy.
- Subsequently, a cold plastic deformation processing was performed using a pilgrim mill set at 70 hits/minute with a feed of 11.11 mm until tubes having a 45mm-diameter by a 2.25-wall thickness were obtained and later the semifinished products obtained thereby were subjected to a single operation of rectilinear cold drawing to a 35mm-diameter by 1.90 mm-thickness and a following annealing at 650°C for 4 hours in a reducing atmosphere. Subsequently, a series of coil drawing operations (to the spinners) were performed up to a 9.52mm-diameter by a 0.45mm-thickness as well as a final annealing at 650°C for 4 hours in a funnel type furnace with a reducing atmosphere. The possible final brushing ensured the absence of surface layers of oxide and/or of layers depleted of Mn.
Claims (4)
- A method for producing articles, these articles being preferably intended to be employed in the health and/or food field, these articles being provided with intrinsic antibacterial properties, the method characterised in that it comprises the steps of:- casting a plate or a cylindrical ingot made of a copper-based alloy containing manganese as the main alloying element, in an amount such as to make the alloy white in colour and to impart a crystalline structure in alpha phase at ambient temperature thereto, wherein said alloy contains manganese in a varying weight percentage between 15% and 40%, optionally up to 2% tin, and does not contain aluminum, and neither zinc, except as impurities, balance copper;- subjecting the plate or ingot to a series of hot plastic deformation machining treatments in sequence, preferable rolling or drawing or extrusion, to obtain a first, predetermined percentage of sectional reduction;- subjecting the hot semifinished article to a series of cold plastic deformation machining treatments in sequence, preferably rolling or drawing, to obtain a second, predetermined percentage of sectional reduction;- subjecting the cold semifinished article thus obtained to one or more heat annealing treatments of complete re-crystallization, in a reducing atmosphere;- subjecting the hot and/or cold semifinished article to at least one step of removing a surface layer thereof with a low manganese content;- subjecting the cold, annealed, semifinished article to a step of abrasive brushing, wherein said step of abrasive brushing is performed so as to remove the surface layer of the cold, annealed, semifinished article having a thickness equal to 4 microns; and- obtaining a desired article with the cold, annealed, semifinished article.
- The method according to claim 1, characterized in that said first and second predetermined percentages of sectional reduction are on the order of 90%.
- The method according to claim 1 or 2, characterized in that said step of complete re-crystallization annealing of the cold semifinished article is performed at a temperature ranging between 550°C and 750°C, in either a static or a tunnel type furnace, and in a reducing atmosphere.
- The method according to anyone of claims from 1 to 3, characterized in that the hot semifinished article is subjected to a step of surface milling for removing the oxidised, low manganese layers.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ITTO2008A000649A IT1392421B1 (en) | 2008-09-01 | 2008-09-01 | USE OF A COPPER-BASED WHITE ALLOY FOR THE PRODUCTION OF NATURALLY ANTI-BACTERIAL PRODUCTS AND THE METHOD FOR THE SAME PRODUCTION OF THEMSELVES |
Publications (2)
Publication Number | Publication Date |
---|---|
EP2161349A1 EP2161349A1 (en) | 2010-03-10 |
EP2161349B1 true EP2161349B1 (en) | 2018-10-17 |
Family
ID=41009891
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP09008026.8A Active EP2161349B1 (en) | 2008-09-01 | 2009-06-19 | Method for producing a copper-based white alloy for producing naturally antibacterial articles |
Country Status (3)
Country | Link |
---|---|
EP (1) | EP2161349B1 (en) |
ES (1) | ES2695752T3 (en) |
IT (1) | IT1392421B1 (en) |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1224937B (en) * | 1963-06-07 | 1966-09-15 | Kurt Dies Dr Ing | Use of copper alloys for objects subject to sliding, friction and wear and a process for producing the same |
US3725052A (en) * | 1969-09-13 | 1973-04-03 | Foundation Res Inst Electric A | Non-magnetic resilient manganese-copper alloy having a substantially temperature-free elastic modulus |
GB1382201A (en) * | 1971-03-03 | 1975-01-29 | Olin Corp | Copper alloy |
JPS6072695A (en) * | 1983-09-28 | 1985-04-24 | Maruyasu Kogyo Kk | Brazing alloy for stainless steel |
JPH08206876A (en) * | 1995-02-02 | 1996-08-13 | Mazda Motor Corp | Brazing method and its brazing filler metal |
DE20006294U1 (en) * | 1999-05-05 | 2000-08-31 | Olin Corporation, Norwalk, Conn. | Copper alloy with a golden appearance |
US6863746B2 (en) | 2001-08-02 | 2005-03-08 | Keith Weinstein | White gold compositions without nickel and palladium |
JP3915889B2 (en) | 2001-10-26 | 2007-05-16 | Ykk株式会社 | Nickel-free white copper alloy and method for producing nickel-free white copper alloy |
EP1880776A1 (en) * | 2006-07-19 | 2008-01-23 | Europa Metalli S.p.A. | Method for the production of tubes |
-
2008
- 2008-09-01 IT ITTO2008A000649A patent/IT1392421B1/en active
-
2009
- 2009-06-19 EP EP09008026.8A patent/EP2161349B1/en active Active
- 2009-06-19 ES ES09008026T patent/ES2695752T3/en active Active
Non-Patent Citations (1)
Title |
---|
None * |
Also Published As
Publication number | Publication date |
---|---|
IT1392421B1 (en) | 2012-03-02 |
EP2161349A1 (en) | 2010-03-10 |
ITTO20080649A1 (en) | 2010-03-02 |
ES2695752T3 (en) | 2019-01-10 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP2728024B1 (en) | Silver-white copper alloy and method for its manufacture | |
EP3056578B1 (en) | Copper alloy | |
EP2952596B1 (en) | Lead-free easy-to-cut corrosion-resistant brass alloy with good thermoforming performance | |
EP2078760A1 (en) | Beta titanium alloy | |
JP5911891B2 (en) | Copper alloy material for seawater and method for producing the same | |
JP5933848B2 (en) | Discoloration-resistant copper alloy and copper alloy member | |
EP2123785A1 (en) | Steel plate having high gathering degree of {222} plane and process for production thereof | |
US4657601A (en) | Thermomechanical processing of beryllium-copper alloys | |
EP2027947A1 (en) | Method for the production of alloy pipes for heat exchangers using precipitation hardening through underwater extrusion | |
CA2712392C (en) | White copper-base alloy | |
KR101796191B1 (en) | Copper alloy with excellent antibiosis, discoloration-resistance and formability, and method for producing same | |
US5501834A (en) | Nonmagnetic ferrous alloy with excellent corrosion resistance and workability | |
JP6477127B2 (en) | Copper alloy rod and copper alloy member | |
EP0992599A1 (en) | Titanium alloy and method for producing the same | |
EP2161349B1 (en) | Method for producing a copper-based white alloy for producing naturally antibacterial articles | |
JP3309769B2 (en) | Cu-containing stainless steel sheet and method for producing the same | |
JPH10306352A (en) | Ferritic stainless steel sheet excellent in antibacterial characteristic and surface characteristic and having high workability, and its production | |
KR102452654B1 (en) | Alloy material with antibacterial activity | |
GB2149819A (en) | Thermomechanical treatment of copper beryllium alloys | |
EP1336665B1 (en) | Cold reduced enamelling steel sheet and an enamelled structure comprising a component of such a steel sheet | |
JPH08225895A (en) | Martensitic stainless steel excellent in antifungal property | |
JPH09118987A (en) | Improvement of antibacterial property for copper containing stainless steel | |
JP2000052062A (en) | Antibacterial plate member and its manufacture | |
EP1950316A1 (en) | Metal material and manufacturing method |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK TR |
|
AX | Request for extension of the european patent |
Extension state: AL BA RS |
|
17P | Request for examination filed |
Effective date: 20100709 |
|
17Q | First examination report despatched |
Effective date: 20100805 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: EXAMINATION IS IN PROGRESS |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: GRANT OF PATENT IS INTENDED |
|
INTG | Intention to grant announced |
Effective date: 20180705 |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE PATENT HAS BEEN GRANTED |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK TR |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: EP |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R096 Ref document number: 602009055068 Country of ref document: DE Ref country code: AT Ref legal event code: REF Ref document number: 1054114 Country of ref document: AT Kind code of ref document: T Effective date: 20181115 |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FG2A Ref document number: 2695752 Country of ref document: ES Kind code of ref document: T3 Effective date: 20190110 |
|
RAP2 | Party data changed (patent owner data changed or rights of a patent transferred) |
Owner name: KME ITALY S.P.A. |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: MP Effective date: 20181017 |
|
REG | Reference to a national code |
Ref country code: LT Ref legal event code: MG4D |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: MK05 Ref document number: 1054114 Country of ref document: AT Kind code of ref document: T Effective date: 20181017 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: NL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181017 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181017 Ref country code: BG Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190117 Ref country code: PL Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181017 Ref country code: HR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181017 Ref country code: LV Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181017 Ref country code: AT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181017 Ref country code: LT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181017 Ref country code: NO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190117 Ref country code: IS Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190217 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190118 Ref country code: PT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20190217 Ref country code: SE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181017 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R097 Ref document number: 602009055068 Country of ref document: DE |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: CZ Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181017 Ref country code: DK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181017 |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181017 Ref country code: EE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181017 Ref country code: RO Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181017 |
|
26N | No opposition filed |
Effective date: 20190718 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SI Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181017 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MC Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181017 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20190619 |
|
REG | Reference to a national code |
Ref country code: BE Ref legal event code: MM Effective date: 20190630 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: TR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181017 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190619 Ref country code: IE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190619 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: BE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190630 Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190619 Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190630 Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20190630 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: CY Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181017 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181017 Ref country code: HU Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO Effective date: 20090619 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MK Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20181017 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: IT Payment date: 20230620 Year of fee payment: 15 Ref country code: ES Payment date: 20230720 Year of fee payment: 15 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20240627 Year of fee payment: 16 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20240625 Year of fee payment: 16 |